N-docosahexaenoyl (4-hydroxyphenyl)-glycine → N-(4-Hydroxyphenyl)glycine
反応式
C([N:22]([C:27]1[CH:32]=[CH:31][C:30]([OH:33])=[CH:29][CH:28]=1)[CH2:23][C:24]([OH:26])=[O:25])(=O)C=CC=CC=CC=CC=CCCCCCCCCC.C(N(C1C=CC(O)=CC=1)CC(O)=O)(=O)C=CC=CC=CC=CC=CC=CCCCCCCCCC>>[OH:33][C:30]1[CH:31]=[CH:32][C:27]([NH:22][CH2:23][C:24]([OH:26])=[O:25])=[CH:28][CH:29]=1参加物
3
実験手順
The same procedure as in Example 5 but EPA-Cl was replaced by 4.2 g (0.012 mole) of the mixture of polyunsaturated fatty acyl chlorides as prepared in Example 4. Yield of the mixed product was about 88 percent, containing N-eicosapentaenoyl (4-hydroxyphenyl)-glycine and N-docosahexaenoyl (4-hydroxyphenyl)-glycine as the main components.
後処理
- customas prepared in Example 4
出典と根拠
- ORDレコード
- ord-180f66a0ac3f4abc9d685a80c62a8443
- 出典データセット
- uspto-grants-1993_06
- 特許番号
- US05216023
反応ノート
読み込み中…